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Prophylactic intervention of spleen ammonia peptide oral solution in patients with allergic rhinitis in Hohhot, Inner Mongolia

Prophylactic intervention of spleen ammonia peptide oral solution in patients with allergic rhinitis in Hohhot, Inner Mongolia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084502
Enrollment
Unknown
Registered
2024-05-17
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

allergic rhinitis

Interventions

Sponsors

Beijing Shijitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: 300 seasonal AR patients in a clinical trial on prevention and treatment of allergic rhinitis in Hohhot, Inner Mongolia in 2023. (1) Age 18-69 years old, male or female; (2) Have a typical history of seasonal allergic rhinitis, and the diagnostic criteria for seasonal AR refer to the Chinese Guidelines for the Diagnosis and Treatment of Allergic Rhinitis (revised edition 2022); ? Symptoms: paroxysmal sneezing, watery nose, nasal itching and nasal congestion and other symptoms appear 2 or more, every day Symptoms lasting or accumulated for more than 1h may be accompanied by eye symptoms such as tearing, eye itching and eye redness. ? Signs: common nasal mucosa pale, edema, nasal watery secretions; Allergen testing in the past or at visit: at least one allergen is positive for SPT and/or serum specific IgE; (3) In patients with pollen allergy, the symptoms were more than 4 weeks in the previous pollen dissemination season, and the average TNSS score of patients before treatment was =6. The average score of nasal congestion symptom was =2, and at least one of the three symptom scores of sneezing, runny nose and itchy nose was =2. (4) Voluntary subjects and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with perennial allergic rhinitis, severe deviation of nasal septum, sinusitis, and nasal polyps; (2) Patients with serious heart, liver, kidney and brain diseases; (3) pregnant and nursing women; (4) Patients with moderate-to-severe asthma who were clearly diagnosed during the pollen season; (5) tricyclic antidepressants, immunosuppressive/immunomodulatory agents, oral hormone drugs were taken 4 weeks before enrollment;

Design outcomes

Primary

MeasureTime frame
The risk of seasonal AR patients after pollen concentration adjustment decreased compared to 2023;

Secondary

MeasureTime frame
symptom score-Four-point method;symptom score-VAS visual analog scale;symptom score-RQLQ Scale;Total drug score;

Countries

China

Contacts

Public ContactWang Xueyan

Beijing Shijitan Hospital, Capital Medical University

Wangxueyan2018@163.com+86 153 0137 8519

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026